Canonical Allele Identifier: CA344143650
Community Standard Title: NM_000069.3(CACNA1S):c.4442-2A>G
Gene: CACNA1S HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201047628T>C , CM000663.2:g.201047628T>C GRCh38
NC_000001.10:g.201016756T>C , CM000663.1:g.201016756T>C GRCh37
NC_000001.9:g.199283379T>C NCBI36
NG_009816.1:g.69939A>G
NG_009816.2:g.69939A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000069.3:c.4442-2A>G MANE Select NP_000060.2:n.4442-2A>G
ENST00000362061.4:c.4442-2A>G MANE Select ENSP00000355192.3:n.4442-2A>G
NM_000069.2:c.4442-2A>G NP_000060.2:n.4442-2A>G
ENST00000362061.3:c.4442-2A>G ENSP00000355192.3:n.4442-2A>G
ENST00000367338.7:c.4385-2A>G ENSP00000356307.3:n.4385-2A>G
ENST00000679417.1:c.*3605-2A>G ENSP00000506706.1:n.*3605-2A>G
ENST00000680051.1:n.1568-2A>G
ENST00000680059.1:c.*1960-2A>G ENSP00000504944.1:n.*1960-2A>G
ENST00000681078.1:c.*217-2A>G ENSP00000506645.1:n.*217-2A>G
ENST00000681190.1:c.*624-2A>G ENSP00000506428.1:n.*624-2A>G
ENST00000681874.1:c.4382-2A>G ENSP00000505162.1:n.4382-2A>G
XM_005245478.2:c.4385-2A>G XP_005245535.1:n.4385-2A>G
XM_005245478.3:c.4385-2A>G XP_005245535.1:n.4385-2A>G